tDCS for Post-Stroke Cognitive Impairment

Recruiting now · Phase 2 · Has a placebo group

Conditions studied: Stroke, Mild Cognitive Impairment

In brief

This study will evaluate the effects of a form of non-invasive brain stimulation on brain functioning and memory in participants with post-stroke cognitive impairment (PSCI).

Key facts

Study ID

NCT06516588

Run by

University of Oklahoma

People needed

80

Starts

2024-09-30

Expected to finish

2027-06-30

Last updated by the study team

2024-10-10

Who can join

Age: 18 and older, up to 99. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• ischemic stroke participants in sub-acute phase (at least 10 days after stroke event or discharge and under 5 months post-event) with cognitive dysfunction (MoCA <26);

You may not qualify if…

• clinically significant or unstable medical or psychiatric condition;
• diagnosis of severe depression;
• history of relevant neurological diagnosis (e.g., epilepsy);
• previous neurosurgical procedure with craniectomy;
• contraindications to tDCS (implanted brain medical devices);
• severe visual impairment, hearing impairment, aphasia, neglect or dementia.

Where it is running

• University of Oklahoma — Oklahoma City, Oklahoma, United States (enrolling)

Full record on ClinicalTrials.gov

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